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rs797044910

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044910(A;G)
Make rs797044910(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87864540
GeneKLLN, PTEN
is asnp
is mentioned by
dbSNPrs797044910
ebirs797044910
HLIrs797044910
Exacrs797044910
Varsomers797044910
Maprs797044910
PheGenIrs797044910
hapmaprs797044910
1000 genomesrs797044910
hgdprs797044910
ensemblrs797044910
gopubmedrs797044910
geneviewrs797044910
scholarrs797044910
googlers797044910
pharmgkbrs797044910
gwascentralrs797044910
openSNPrs797044910
23andMers797044910
23andMe allrs797044910
SNP Nexus

SNPshotrs797044910
SNPdbers797044910
MSV3drs797044910
GWAS Ctlgrs797044910
Max Magnitude0
ClinVar
Risk rs797044910(G;G)
Alt rs797044910(G;G)
Reference rs797044910(A;A)
Significance Pathogenic
Disease Inborn genetic diseases PTEN hamartoma tumor syndrome
Variation info
Gene PTEN LOC101929706 KLLN
CLNDBN Inborn genetic diseases PTEN hamartoma tumor syndrome
Reversed 0
HGVS NC_000010.10:g.89624297A>G
CLNSRC
CLNACC RCV000190739.1, RCV000234212.1,